Gee-Chen ChangDavid Chi-Leung LamChun-Ming TsaiYuh-Min ChenJin-Yuan ShihShyam AggarwalShuhang WangSang-We KimYoung-Chul KimIbrahim WahidRubi LiDarren Wan-Teck LimVirote SriuranpongRaymond Tsz-Tong ChanRobert M. LorencePhilippe CarriereChristina RaabeAgnieszka CsehKeunchil Park2026-01-302026-01-302021-03-3010.1007/s10147-021-01869-0https://scholars.csmu.edu.tw/handle/123456789/4142<jats:title>Abstract</jats:title><jats:sec> <jats:title>Background</jats:title> <jats:p>This study evaluated outcomes among patients with advanced/metastatic non-small-cell lung cancer (NSCLC) treated at Asian centers participating in the global named-patient-use (NPU) program for afatinib.</jats:p> </jats:sec><jats:sec> <jats:title>Methods</jats:title> <jats:p>Patients had progressed after initial benefit with erlotinib or gefitinib, and/or had an <jats:italic>EGFR</jats:italic> or <jats:italic>HER2</jats:italic> mutation, had no other treatment options, and were ineligible for afatinib trials. The recommended starting dose of afatinib was 50 mg/day. Dose modifications were allowed, and afatinib was continued as long as deemed beneficial. Response and survival information was provided voluntarily. Safety reporting was mandatory.</jats:p> </jats:sec><jats:sec> <jats:title>Results</jats:title> <jats:p>2242 patients (26% aged ≥ 70 years, 96% with adenocarcinoma) received afatinib at centers in 10 Asian countries. Most were heavily pre-treated, including prior treatment with erlotinib or gefitinib. Of 1281 patients tested, 1240 had <jats:italic>EGFR</jats:italic> mutations (common: 1034/1101; uncommon: 117/1101). There were no new safety signals, the most common adverse events being rash and diarrhea. Objective response rate (ORR) was 24% overall (<jats:italic>n</jats:italic> = 431 with data available), 27% for patients with common <jats:italic>EGFR</jats:italic> mutations (<jats:italic>n</jats:italic> = 230) and 28% for those with uncommon mutations (<jats:italic>n</jats:italic> = 32); median time to treatment failure (TTF) in these groups was 7.6 months (<jats:italic>n</jats:italic> = 1550), 6.4 months (<jats:italic>n</jats:italic> = 692) and 8.4 months (<jats:italic>n</jats:italic> = 83), respectively. In patients with <jats:italic>EGFR</jats:italic> exon 20 insertions (<jats:italic>n</jats:italic> = 23) and <jats:italic>HER2</jats:italic> mutations (<jats:italic>n</jats:italic> = 12), median TTF exceeded 12 months.</jats:p> </jats:sec><jats:sec> <jats:title>Conclusions</jats:title> <jats:p>Patient outcomes in this study were similar to those reported in the analysis of the global NPU. Afatinib achieved clinical benefits in patients with refractory NSCLC. ORR and TTF were similar between patients with tumors harboring uncommon and common <jats:italic>EGFR</jats:italic> mutations.</jats:p> </jats:sec>[SDGs]SDG3journal-article